Canonical Allele Identifier: CA1955169906

Gene: USH1C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17494415T= , CM000673.2:g.17494415T=	GRCh38
NC_000011.9:g.17515962T= , CM000673.1:g.17515962T=	GRCh37
NC_000011.8:g.17472538T=	NCBI36
NG_011883.1:g.55002A=
NG_011883.2:g.55002A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000005226.12:c.2656-39A= MANE Select	ENSP00000005226.7:n.2656-39A=
ENST00000318024.9:c.1647-39A= MANE Plus Clinical	ENSP00000317018.4:n.1647-39A=
ENST00000005226.11:c.2656-39A=	ENSP00000005226.7:n.2656-39A=
ENST00000318024.8:c.1647-39A=	ENSP00000317018.4:n.1647-39A=
ENST00000526313.5:c.*361-39A=	ENSP00000432236.1:n.*361-39A=
ENST00000527020.5:c.1590-39A=	ENSP00000436934.1:n.1590-39A=
ENST00000527551.1:n.157-39A=
ENST00000527720.5:c.1554-39A=	ENSP00000432944.1:n.1554-39A=
ENST00000529563.5:n.531-39A=
ENST00000624811.1:n.679A=
NM_001297764.1:c.1590-39A=	NP_001284693.1:n.1590-39A=
NM_005709.3:c.1647-39A=	NP_005700.2:n.1647-39A=
NM_153676.3:c.2656-39A=	NP_710142.1:n.2656-39A=
NR_123738.1:n.1682-39A=
XM_011519831.1:c.2571-39A=	XP_011518133.1:n.2571-39A=
XM_011519832.1:c.1800-39A=	XP_011518134.1:n.1800-39A=
XM_011519832.3:c.1800-39A=	XP_011518134.1:n.1800-39A=
XM_017017075.1:c.*938A=	XP_016872564.1:n.*938A=
XR_001747717.2:n.1806-39A=
NM_153676.4:c.2656-39A= MANE Select	NP_710142.1:n.2656-39A=
NM_001297764.2:c.1590-39A=	NP_001284693.1:n.1590-39A=
NM_005709.4:c.1647-39A= MANE Plus Clinical	NP_005700.2:n.1647-39A=
NR_123738.2:n.1682-39A=